Conversion of unsaturated fatty acids-nucleophilic additions to methyl (E)-12-oxo-10-octadecenoate [1]
- Author
- MALETZ, R; SCHÄFER, H. J; QUERMANN, R1
[1] Organisch-Chemisches Institut der Universität Münster, Germany - Source
Fett (Weinheim). = Lipid. 1996, Vol 98, Num 11, pp 370-379 ; ref : 37 ref
- CODEN
- FWTEEG
- ISSN
- 0931-5985
- Scientific domain
- Food science technology; Chemical industry parachemical industry
- Publisher
- Wiley-VCH, Weinheim
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide gras insaturé Addition nucléophile Composé aliphatique Composé éthylénique Cétoacide Hydroxyacide Oxydation Réactivité chimique Stéréoisomère trans Synthèse chimique Octadéc-10-énoïque acide(12-oxo) ester méthyle Ricinoléique acide ester méthyle
- Keyword (en)
- Unsaturated fatty acid Nucleophilic addition Aliphatic compound Ethylenic compound Ketoacid Hydroxyacid Oxidation Chemical reactivity Trans stereoisomer Chemical synthesis
- Keyword (es)
- Acido graso no saturado Adición nucleófila Compuesto alifático Compuesto etilénico Cetoácido Hidroxiácido Oxidación Reactividad química Estereoisómero trans Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C02 Aliphatic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2516970
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/lipi.19960981106 
https://dx.doi.org/10.1002/lipi.19960981106
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